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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
LILRA4
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
CNOT3, LAIR1
+18 more
Copy number gain
not provided
GUncertain significance
LAIR1, LILRA3
+4 more
Copy number gain
not provided
GUncertain significance
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